chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1156200949156200950AG20GENIChomozygous135716288
1156201151156201152CT18GENIChomozygous141265615
1156201464156201465C14GENIChomozygous141172457
1156201644156201645TC13GENIChomozygous135716289
1156202758156202759AT7GENIChomozygous135716290
1156203408156203409GA11GENIChomozygous141265616
1156203776156203777GA9GENIChomozygous141265617
1156204376156204377CT13GENIChomozygous135716292
1156204661156204662GA16GENIChomozygous135716293
1156205781156205782CT17GENIChomozygous141265618
1156206431156206432TG16GENIChomozygous135716294
1156210741156210742AG17GENIChomozygous135716296
1156210753156210754GA15GENIChomozygous135716297
1156214704156214705CG15GENIChomozygous135716299
1156216263156216264CT10GENIChomozygous135716300
1156216982156216983TC18GENIChomozygous135716301
1156213435156213436A3GENIChomozygous140958709
1156205454156205455CA5GENICheterozygous402969229
1156205454156205455C5GENIChomozygous402969228